피브린 실란트의 코성형술 후 합병증 감소 효과: 메타분석

The Efficacy of Fibrin Sealant to Reduce Complications After Rhinoplasty: A Meta-Analysis

Article information

Korean J Otorhinolaryngol-Head Neck Surg. 2024;67(1):22-27
Publication date (electronic) : 2023 July 6
doi : https://doi.org/10.3342/kjorl-hns.2022.01130
1Department of Otorhinolaryngology-Head and Neck Surgery, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang, Korea
2Department of Otorhinolaryngology-Head and Neck Surgery, Kyung Hee University Hospital at Gangdong, College of Medicine, Kyung Hee University, Seoul, Korea
강정욱1orcid_icon, 방제호2orcid_icon, 손승엽2, 이건희,2orcid_icon
1한림대학교 의과대학 성심병원 이비인후과학교실
2경희대학교 의과대학 강동경희대학교병원 이비인후과학교실
Address for correspondence Kun Hee Lee, MD, PhD Department of Otorhinolaryngology-Head and Neck Surgery, Kyung Hee University Hospital at Gangdong, College of Medicine, Kyung Hee University, 892 Dongnam-ro, Gangdong-gu, Seoul 05278, Korea Tel +82-2-440-6181 Fax +82-2-440-7336 E-mail nose4u@gmail.com
Received 2022 November 30; Revised 2023 March 10; Accepted 2023 March 20.

Trans Abstract

Background and Objectives

Fibrin sealant (FS) is widely used to reduce postoperative bleeding. This analysis aimed to assess the efficacy of FS to reduce complications after rhinoplasty.

Materials and Method

We searched PubMed, Scopus, Embase, the Cochrane Library, and the Web of Science database for articles on FS and rhinoplasty from the inception of publication to December 29, 2021. Post-rhinoplasty complications, such as edema and ecchymosis, were recorded. The final meta-analysis was performed using three studies.

Results

Two subgroups were created based on the FS usage after rhinoplasty. The FS effect on edema reduction was favorable on the postoperative day-1 (standardized mean difference [SMD]=-1.07 [-1.70; -0.45]). In addition, the FS effect on ecchymosis reduction was favorable on the postoperative day-1 postoperative (SMD=-1.33 [-2.15; -0.50]).

Conclusion

Our study shows that FS reduces the early complications of rhinoplasty.

Introduction

According to the American Society of Plastic Surgeons cohort study, facial plastic surgery is steadily increasing with the growth of the gross domestic product [1]. In particular, the rhinoplasty rate is second only to the rate of minimally invasive cosmetic surgeries [1]. Although rhinoplasty is considered a cosmetic surgery, complications such as edema and ecchymosis frequently occur after the procedure. Such complications aggravate patient discomfort and delay a return to daily life. Consequently, various therapeutic methods such as steroids, intraoperative hypotension, intraoperative cooling, head elevation, piezosurgery, and tranexamic acid have been tested to reduce morbidities after rhinoplasty [2-5]. Some of these treatments are known to reduce postoperative morbidities, but some remain controversial [4]. Despite considerable effort, edema and ecchymosis are still frequent after rhinoplasty, and are a major cause of deterioration in patient quality of life. Moreover, severe edema and ecchymosis can increase scarring and alter intended surgical outcomes [6,7].

Surgical method characteristics can also affect postoperative morbidities. The surgical techniques used in rhinoplasty are classified into open (external) rhinoplasty and closed (endonasal) rhinoplasty [8]. Endonasal rhinoplasty is associated with low morbidities and results in a natural appearance. This outcome is achieved by retaining the original shape of the nose and preserving major cartilage architectures. However, endonasal rhinoplasty has disadvantages as it is a difficult surgical technique, provides limited visibility, and allows inadequate accessibility to cartilage. On the other hand, open rhinoplasty is a more straightforward method for accessing cartilage, and is preferred for highly complex surgeries and educational purposes. However, open rhinoplasty also has disadvantages including a high complication rate and delayed recovery time. High postoperative morbidities might be expected because soft tissue bleeding is inevitable due to the nature of external rhinoplasty. In particular, it is known that osteotomy, which is frequently performed in rhinoplasty, increases morbidities such as edema and ecchymosis [9]. Because open rhinoplasty and osteotomy cannot be completely avoided, methods to reduce postoperative morbidities more effectively are needed.

Fibrin sealant (FS) is a plasma cryoprecipitate-based sealant that consists of two components: human sealer protein and human thrombin [10]. The invention of this sealant was based on the development of the fibrin network that represents the final phase in the blood coagulation process. Morawitz [11] was the first to describe the physiological mechanism of FS. Since it was invented, FS has been widely used for suture support, tissue adhesion, and hemostasis. Several studies have shown that FS reduces postoperative bleeding and ecchymosis by sealing capillary vessels, which in turn lessens postoperative swelling by promoting wound adhesion and minimizing dead space [12,13]. Recently, attempts were made to test the efficacy of FS to reduce postoperative complications after rhinoplasty. Consequently, the purpose of this meta-analysis was to investigate whether the application of FS could reduce the severity of complications such as edema and ecchymosis after rhinoplasty. We reviewed randomized controlled trials (RCTs) that compared the rate of complications after rhinoplasty between patients who were treated with FS, and those who were not.

Materials and Methods

Protocol and registration

This study was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) statement [14].

Selection criteria

Only RCTs comparing patients (≥18 years) who underwent open rhinoplasty with or without osteotomy, and with or without FS treatment were included in this review. The outcomes of interest were postoperative edema (swelling) and ecchymosis (bruising) of the nose and eyes.

Search strategy

PubMed, Scopus, Embase, The Cochrane Library, and Web of Science databases were searched to retrieve indexed articles for this study. Articles published in languages other than English were excluded. The final search was conducted on December 29, 2021. The basic search expressions were as follows: (rhinoplasty OR osteotomy) AND (fibrin OR fibrin glue OR fibrin sealant) AND (edema OR swelling OR bruise OR ecchymosis) AND randomized controlled trial. We also considered alternative spellings and abbreviations in the database search process. Relevant reviews were also manually searched and assessed to identify any dropped articles in the search process.

Data extraction and quality assessment

The full article texts were independently evaluated twice for eligibility by review authors. Disagreements were resolved by consensus through discussion among the authors, JWK and KHL. The collected data were as follows: first author’s name, publication year, study design, number of patients, mean age of the patients, type of control group, osteotomy conduction, type of FS, time of follow-up, and outcomes. The bias and quality of the RCTs were assessed using RevMan 5, which is a Cochrane Collaboration tool. The domains of assessment were as follows: random sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome data, selective reporting, and other biases. The domains were rated by three grades: high risk, low risk, and unclear risk of bias.

Measures of postoperative outcome

Since heterogeneity exists in meta-analyses of postoperative outcome data, a random effects model was used for meta-analysis with data from the included RCTs. The relative risks for assessment scales of postoperative outcomes were calculated as the standard mean differences. Ninety-five percent confidence intervals were used for statistical significance. Statistical analyses were conducted using R software (version 4.1.0) with the meta and metaphor packages.

Results

Study selection and characteristics

A total of 26 studies were retrieved using the search expressions to query the five databases (Fig. 1), and 16 duplicates were subsequently excluded. Detailed numbers of studies at each stage are described in the PRISMA flowchart (Fig. 1). Five studies were excluded after screening the titles and abstracts. Two studies were excluded from the eligibility process due to the absence of appropriate outcome data. Finally, the three remaining eligible studies were analyzed in this meta-analysis study [13,15,16].

Fig. 1.

PRISMA flow chart.

Study characteristics

The characteristics of the included studies are presented in Table 1. The total number of subjects in all the studies was 60, with a mean age of 35.1 years. In the study by Pryor, et al. [13], 10 participants underwent application of FS on one side and not on the contralateral side, and the postoperative complications were compared between the two sides. In another study by Yu, et al. [15], 41 participants underwent rhinoplasty without osteotomy in Korea. In other studies, 19 participants underwent rhinoplasty in the United States. All the studies measured edema and ecchymosis of the nose and eyelid on day-1 and at 1-week postoperatively. A five-level grading scale was used for the 41 participants in the Yu, et al. [15] study. Two other studies applied a 10 cm visual analog scale to evaluate the severity of postoperative edema and ecchymosis complications.

Summary of studies included in the meta-analysis

Risk of bias within studies

The quality of the three studies was assessed using Rev-Man 5, which is recommended by the Cochrane Collaboration to determine risk of bias. A summary of the assessment is presented in Fig. 2. Participant blindness was generally maintained because patients could not know whether FS was applied or not. However, selection and detection bias could not be fully assessed in the first two studies shown in Fig. 2 due to a lack of detailed descriptions. We found considerable variation in the quality of the included studies, which ranged from low to good quality (Fig. 2). One of the three RCTs (Yu, et al. [15] has good reliability, while the other (Dayan, et al. [16]) has high bias, low reliability, and a small sample size. Hence, the findings of Yu, et al. [15] and Pryor, et al. [13] more influence the conclusions of this study than that of Dayan, et al. [16]

Fig. 2.

Risk of bias assessment. A: Risk of bias and applicability concerns graph. B: Risk of bias and applicability concerns summary.

Postoperative edema

Fig. 3 shows a forest plot for edema severity with or without FS application on day-1 and at 1-week postoperative. A heterogeneity analysis revealed I2 values of 25% (p=0.26) on day-1 and 0% (p=0.66) at 1-week postoperative, indicating no significant heterogeneity. On day-1 postoperative, two studies showed reduced edema severity after FS application (Pryor, et al. [13], standardized mean difference [SMD]=-1.11 [-2.07; -0.15], Yu, et al. [15], SMD=-1.40 [-2.09; -0.71]). At 1-week postoperative, all studies failed to show any FS effectiveness. The overall pooled effect of FS in reducing edema was favorable only on day-1 postoperative (SMD=-1.07 [-1.70; -0.45]), and not at 1-week postoperative (SMD=-0.40 [-0.88; 0.07]).

Fig. 3.

Forest plot of edema after rhinoplasty with or without FS application. A: Edema on day-1 after rhinoplasty. B: Edema 1 week after rhinoplasty. SD, standard deviation; SMD, standardized mean difference; CI, confidence interval.

Postoperative ecchymosis

Similar to Figs. 3 and 4 shows the severity of ecchymosis with or without FS application on day-1 and at 1-week postoperative. A heterogeneity analysis of ecchymosis severity revealed I2 values of 48% (p=0.15) on day-1 and 75% (p=0.02) at 1-week postoperative. On day-1 postoperative, two studies showed reduced ecchymosis severity after FS application (Pryor, et al. [13], SMD=-2.24 [-3.41; -1.07], Yu, et al. [15], SMD=-1.18 [-1.85; -0.51]). At 1-week postoperative, only one study showed favorable outcomes after FS application (Pryor, et al. [13], SMD=-1.31 [-2.30; -0.32]). The overall pooled effect for FS reduction of ecchymosis was also favorable only on day-1 (SMD=-1.33 [-2.15; -0.50]), and not at 1-week (SMD=-0.16 [-1.28; 0.95]) postoperative.

Fig. 4.

Forest plot of ecchymosis after rhinoplasty with or without FS application. A: Ecchymosis on day-1 after rhinoplasty. B: Ecchymosis 1 week after rhinoplasty. SD, standard deviation; SMD,standardized mean difference; CI, confidence interval.

Discussion

Various studies have attempted to identify the benefits and side effects of FS application in otolaryngology. A previous study of 100 parotidectomy patients confirmed that application of FS caused very few side effects [17]. Another report showed that FS could replace drainage in thyroidectomy [18,19]. Other surgical uses for FS include reduction of the transfusion rate in femoral neck fractures and knee surgeries [20,21]. An additional study confirmed that FS reduced the risk of leakage in laparoscopic common bile duct incision [22].

Postoperative edema and ecchymosis are the most common side effects of rhinoplasty. Meticulous techniques and standard hemostasis are crucial and cannot be replaced by hemostatics. However, the surgical field of rhinoplasty is very narrow and commonly involves soft tissue and bony destruction. These features allow surgeons performing rhinoplasty to use an applicable hemostatic method. The main purpose of this study was to evaluate whether FS could reduce complications frequently occurring in patients who undergo rhinoplasty. We analyzed three RCTs that studied the effects of FS on the rate of postoperative complications.

The adhesive, sealing, and hemostatic properties of FS may be useful in rhinoplasty. FS can reduce capillary bleeding and serous exudate at the operative site. Two of the three studies included in this meta-analysis demonstrated an advantage associated with FS application on day-1 after rhinoplasty. An FS effect on the reduction of complications was observed only during the initial few days after surgery and not at 1-week postoperative. This outcome could be due to the gradual recovery over time of patients without FS application. The results from this study showed that the application of FS reduced early capillary bleeding and exudate. Considering that patient discomfort is severe in the initial period just after surgery, we expect that the use of FS will be acceptable. An additional advantage for patients is a possible early return to daily life and work. Furthermore, it is encouraging that the three studies analyzed in this meta-analysis did not report any serious side effects, such as allergic reactions to FS.

Our study has several limitations. First, the number of papers and participants in this meta-analysis is small, and the sample size is skewed toward a single paper. Second, the three RCTs have distinct designs, and some of them deviate slightly from the RCT standard. Thus, interpretation requires prudence. However, to the best of our knowledge, this is the first meta-analysis to assess the effects of FS in preventing rhinoplasty-associated morbidities, including ecchymosis and edema.

In conclusion, FS significantly reduced 1-day postoperative complications such as ecchymosis and edema in patients who underwent rhinoplasty. Further large-scale studies on the efficacy of FS to reduce surgical complications after rhinoplasty are needed.

Acknowledgements

None

Notes

Author Contribution

Conceptualization: Kun Hee Lee. Data curation: Jeong Wook Kang, Je Ho Bang. Formal analysis: Jeong Wook Kang. Investigation: Jeong Wook Kang, Je Ho Bang. Methodology: Kun Hee Lee. Project administration: Jeong Wook Kang, Seung Yup Son. Supervision: Kun Hee Lee. Writing—original draft: Jeong Wook Kang, Kun Hee Lee. Writing—review & editing: Jeong Wook Kang, Je Ho Bang, Kun Hee Lee.

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Article information Continued

Fig. 1.

PRISMA flow chart.

Fig. 2.

Risk of bias assessment. A: Risk of bias and applicability concerns graph. B: Risk of bias and applicability concerns summary.

Fig. 3.

Forest plot of edema after rhinoplasty with or without FS application. A: Edema on day-1 after rhinoplasty. B: Edema 1 week after rhinoplasty. SD, standard deviation; SMD, standardized mean difference; CI, confidence interval.

Fig. 4.

Forest plot of ecchymosis after rhinoplasty with or without FS application. A: Ecchymosis on day-1 after rhinoplasty. B: Ecchymosis 1 week after rhinoplasty. SD, standard deviation; SMD,standardized mean difference; CI, confidence interval.

Table 1.

Summary of studies included in the meta-analysis

Study, year Study type Sample size (M/F) Mean age (range) years Control Osteotomy fashion Type of fibrin sealant Measured outcome
Dayan, et al. [16], 2018 RCT 9 (2/7) None (18-50) Other patients who underwent rhinoplasty High-low-high ARTISS, human, aerosolized type Edema, ecchymosis, recovery time, satisfaction
Pryor, et al. [13], 2008 RCT 10 (5/5) 41 (21-66) Contralateral side of the same patient Bilateral osteotomy Evicel, human; Johnson & Johnson–Wound Management, Somerville, Swelling, bruising
Yu, et al. [15], 2018 RCT 41 (28/13) 33.6 (none) Other patients who underwent rhinoplasty Not conducted New Jersey Aerosolized type Periorbital ecchymosis, eyelid edema, dorsal/tip edema

RCT, randomized controlled trial